Bryan Smith, associate professor of biomedical engineering at MSU,
and a team of scientists created a "Trojan Horse" nanoparticle that can
be directed to eat debris, reducing and stabilizing plaque. The
discovery could be a potential treatment for atherosclerosis, a leading
cause of death in the United States.
The results, published in the current issue of Nature Nanotechnology,
showcases the nanoparticle that homes in on atherosclerotic plaque due
to its high selectivity to a particular immune cell type -- monocytes
and macrophages. Once inside the macrophages in those plaques, it
delivers a drug agent that stimulates the cell to engulf and eat
cellular debris. Basically, it removes the diseased/dead cells in the
plaque core. By reinvigorating the macrophages, plaque size is reduced
and stabilized.
Smith said that future clinical trials on the nanoparticle are
expected to reduce the risk of most types of heart attacks, with minimal
side effects due to the unprecedented selectivity of the nanodrug.
Smith's studies focus on intercepting the signaling of the receptors
in the macrophages and sending a message via small molecules using
nano-immunotherapeutic platforms. Previous studies have acted on the
surface of the cells, but this new approach works intracellularly and
has been effective in stimulating macrophages.
"We found we could stimulate the macrophages to selectively eat dead
and dying cells -- these inflammatory cells are precursor cells to
atherosclerosis -- that are part of the cause of heart attacks," Smith
said. "We could deliver a small molecule inside the macrophages to tell
them to begin eating again."
This approach also has applications beyond atherosclerosis, he added.
"We were able to marry a groundbreaking finding in atherosclerosis by
our collaborators with the state-of-the-art selectivity and delivery
capabilities of our advanced nanomaterial platform. We demonstrated the
nanomaterials were able to selectively seek out and deliver a message to
the very cells needed," Smith said. "It gives a particular energy to
our future work, which will include clinical translation of these
nanomaterials using large animal models and human tissue tests. We
believe it is better than previous methods."
Smith has filed a provisional patent and will begin marketing it later this year.
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